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  1. AU=Sperling Brita
  2. AU="Koscianski, Christina A"
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  1. Article: Synovial chondromatosis and chondrosarcoma: a diagnostic dilemma.

    Sperling, Brita L / Angel, Steven / Stoneham, Grant / Chow, Vance / McFadden, Andrew / Chibbar, Rajni

    Sarcoma

    2008  Volume 7, Issue 2, Page(s) 69–73

    Abstract: Purpose: The progression of synovial chondromatosis to chondrosarcoma is very rare. Distinction between these two entities may be difficult on histology alone, and should be based on clinical, radiographic and microscopic evidence. Immunohistochemical ... ...

    Abstract Purpose: The progression of synovial chondromatosis to chondrosarcoma is very rare. Distinction between these two entities may be difficult on histology alone, and should be based on clinical, radiographic and microscopic evidence. Immunohistochemical markers that would facilitate differentiation between synovial chondromatosis and chondrosarcoma are currently being investigated.
    Patients: We describe the cases of two patients who presented with synovial chondromatosis and progression to synovial chondrosarcoma during periods of 7 and 11 years. Several biopsies and resected specimens demonstrated synovial chondromatosis before a diagnosis of chondrosarcoma was made.
    Method: We have examined five markers (Bcl2, Ki67, p27, p16, and p53) in all specimens from these cases, as well as known cases of chondromatosis and chondrosarcoma for control purposes.
    Results: We found increased expression of Bcl2 in benign chondromatosis compared to synovial or central chondrosarcomas.
    Discussion: Distinction between chondromatosis and its progression to low grade chondrosarcoma is difficult at histological level, and must involve incorporation of clinical and radiographical data. Although preliminary, our study suggests that reduced or absent expression of Bcl2 is associated withmalignant transformation of chondromatosis.
    Language English
    Publishing date 2008-06-03
    Publishing country Egypt
    Document type Journal Article
    ZDB-ID 1338527-6
    ISSN 1357-714X
    ISSN 1357-714X
    DOI 10.1080/13577140310001607293
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Microscopic pulmonary tumour embolism: an unusual presentation of thymic carcinoma.

    Sperling, Brita L / Cockcroft, Donald W / Chibbar, Rajni

    Canadian respiratory journal

    2002  Volume 9, Issue 5, Page(s) 347–350

    Abstract: The present report describes the first reported case of microscopic pulmonary tumour embolism (MPTE) from thymic carcinoma. The carcinoma was discovered during an autopsy in a 55-year-old man who had undergone surgery for a pilonidal sinus two weeks ... ...

    Abstract The present report describes the first reported case of microscopic pulmonary tumour embolism (MPTE) from thymic carcinoma. The carcinoma was discovered during an autopsy in a 55-year-old man who had undergone surgery for a pilonidal sinus two weeks before presentation. Pulmonary thromboembolism was suspected. This case was unusual because MPTE has never before been associated with thymic carcinoma, MPTE was the first clinical indication of an occult malignancy, and the clinical presentation was that of sudden onset of dyspnea associated with acute cor pulmonale. The cause of death was determined to be hypoxia secondary to extrinsic compression of the right pulmonary artery and extensive tumour emboli in the small arteries, arterioles and venules of the pulmonary parenchyma. A review of the clinical presentation and diagnosis of MPTE is included.
    MeSH term(s) Fatal Outcome ; Humans ; Immunohistochemistry ; Lung Neoplasms/metabolism ; Lung Neoplasms/secondary ; Male ; Middle Aged ; Neoplastic Cells, Circulating/metabolism ; Neoplastic Cells, Circulating/pathology ; Pilonidal Sinus/surgery ; Postoperative Complications ; Pulmonary Heart Disease/etiology ; Thymus Neoplasms/metabolism ; Thymus Neoplasms/pathology
    Language English
    Publishing date 2002-09
    Publishing country Egypt
    Document type Case Reports ; Journal Article
    ZDB-ID 1213103-9
    ISSN 1916-7245 ; 1198-2241
    ISSN (online) 1916-7245
    ISSN 1198-2241
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Thymoma: a review of the clinical and pathological findings in 65 cases.

    Sperling, Brita / Marschall, Jeff / Kennedy, Renee / Pahwa, Punam / Chibbar, Rajnl

    Canadian journal of surgery. Journal canadien de chirurgie

    2003  Volume 46, Issue 1, Page(s) 37–42

    Abstract: Introduction: Although rare, thymoma is the most common tumour of the anterior mediastinum. In an effort to assess the clinical and pathologic characteristics of this tumour and to determine whether clinicopathologic stage or histopathologic ... ...

    Abstract Introduction: Although rare, thymoma is the most common tumour of the anterior mediastinum. In an effort to assess the clinical and pathologic characteristics of this tumour and to determine whether clinicopathologic stage or histopathologic classification correlates with clinical outcome, in the Department of Pathology and the Department of Surgery at the University of Saskatchewan we reviewed all cases of thymoma registered in the province of Saskatchewan using the database of the Saskatchewan Cancer Centre.
    Methods: In 65 patients with a diagnosis of thymoma or thymic carcinoma identified from the Saskatchewan Cancer Centre database between Jan. 1, 1960, and Dec. 31, 2000, we studied the presentation, diagnostic investigations, therapeutic interventions, tumour size, postoperative course, clinical stage, histopathologic classification, disease recurrence and mortality.
    Results: Of the 65 patients, 17 (26%) were asymptomatic and 11 (17%) had symptoms consistent with myasthenia gravis. Surgical resection is most commonly performed through a median sternotomy and frequently requires en bloc resection of one or more adjacent structures. The overall survival of patients with thymomawas found to correlate with the clinical stage as described by Masaoka and colleagues and with complete tumour resection. A trend to clinicopathologic correlation was observed when applying the histologic classification systems of Suster and Moran and the World Health Organisation, but this trend was not statistically significant.
    Conclusions: Thymoma is a rare tumour with a variable clinical presentation. Clinical outcome correlates with clinical stage and the ability to achieve complete tumour resection.
    MeSH term(s) Adult ; Aged ; Female ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Survival Analysis ; Thymectomy ; Thymoma/diagnosis ; Thymoma/mortality ; Thymoma/pathology ; Thymoma/surgery ; Thymus Neoplasms/diagnosis ; Thymus Neoplasms/mortality ; Thymus Neoplasms/pathology ; Thymus Neoplasms/surgery
    Language English
    Publishing date 2003-02
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 410651-9
    ISSN 0008-428X
    ISSN 0008-428X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Synovial Chondromatosis and Chondrosarcoma

    Andrew M c Fadden / Rajni Chibbar / Vance Chow / Steven Angel / Grant Stoneham / Brita L. Sperling

    Sarcoma, Vol 7, Iss 2, Pp 69-

    A Diagnostic Dilemma

    2003  Volume 73

    Keywords Neoplasms. Tumors. Oncology. Including cancer and carcinogens ; RC254-282 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Oncology ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language English
    Publishing date 2003-01-01T00:00:00Z
    Publisher Hindawi Publishing Corporation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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